rs1060499799

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1060499799(G;T)

Make rs1060499799(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

75844977

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs1060499799
dbSNP (classic)	rs1060499799
ClinGen	rs1060499799
ebi	rs1060499799
HLI	rs1060499799
Exac	rs1060499799
Gnomad	rs1060499799
Varsome	rs1060499799
LitVar	rs1060499799
Map	rs1060499799
PheGenI	rs1060499799
Biobank	rs1060499799
1000 genomes	rs1060499799
hgdp	rs1060499799
ensembl	rs1060499799
geneview	rs1060499799
scholar	rs1060499799
google	rs1060499799
pharmgkb	rs1060499799
gwascentral	rs1060499799
openSNP	rs1060499799
23andMe	rs1060499799
SNPshot	rs1060499799
SNPdbe	rs1060499799
MSV3d	rs1060499799
GWAS Ctlg	rs1060499799

Max Magnitude

0

ClinVar
Risk	rs1060499799(T;T)
Alt	rs1060499799(T;T)
Reference	Rs1060499799(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO6
CLNDBN	Deafness, autosomal dominant 22
Reversed	0
HGVS	NC_000006.11:g.76554694G>T
CLNSRC
CLNACC	RCV000454125.1,